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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **5326 - 5350** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:0070272	hereditary nonpolyposis colorectal cancer type 5 Aliases: HNPCC5	Msh6	17688	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110545	autosomal dominant nonsyndromic deafness 13 Aliases: DFNA13 autosomal dominant deafness 13	Col11a2	12815	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13550	angle-closure glaucoma Aliases: ACG - Angle-closure glaucoma Angle Closure Glaucoma Closed angle glaucoma Narrow cleft glaucoma primary open-angle glaucoma with narrow angles	Hgf Mmp9 Muc5ac Nos3 Tfap2b	15234 17395 17833 18127 21419	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080249	erythrokeratodermia variabilis et progressiva 3	Gja1	14609	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1962	fallopian tube disease	Ccr5	12774	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2754	glycogen storage disease VI Aliases: Glycogen storage disease 6 Hers' disease glycogen storage disease type VI hepatic glycogen phosphorylase deficiency hepatophosphorylase deficiency glycogenosis	Pygl	110095	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050869	villous adenoma	Rnf43	207742	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110480	autosomal recessive nonsyndromic deafness 22 Aliases: DFNB22 autosomal recessive deafness 22	Otoa	246190	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070393	developmental and epileptic encephalopathy 107 Aliases: DEE107 early infantile epileptic encephalopathy 107	Napb	17957	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:439	neuromuscular junction disease	Idh3a Syt1 Syt2	20979 20980 67834	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9119	acute myeloid leukemia Aliases: AML - acute Myeloid Leukemia Leukemia, Myelocytic, acute acute myeloblastic leukaemia acute myeloblastic leukemia acute myelogenous leukaemia acute myelogenous leukemia acute myeloid leukaemia	Abcc3 Abcg2 Abl1 Asxl1 Calr Cbl Ccl2 Cd86 Cdh1 Cfhr1 Chi3l1 Csf2 Csf3 Csf3r Ctla4 Cxcr4 Cyp1a1 Dnmt1 Ephx1 Ezh2 F3 Fanca Fas Fermt2 Fgfr1 Flt3 Gpi1 Gpx1 Gsr H2-Ab1 Idh1 Idh2 Il10 Il1a Itgav Itgb3 Kit Kras Lpp Mllt10 Ncoa2 Nf1 Nos3 Npm1 Nup214 Nup98 Picalm Sh3gl1 Sod2 Tet2 Tfpi2 Tfr2 Tnfsf9 Top2a Top2b Trp53 Vegfa	11350 12317 12402 12477 12524 12550 12654 12767 12981 12985 12986 13076 13433 13849 14056 14066 14087 14102 14182 14255 14751 14775 14782 14961 15926 16153 16175 16410 16416 16590 16653 17354 17978 18015 18127 18148 20296 20405 20656 210126 214133 21789 218952 21950 21973 21974 22059 22339 227720 228790 233489 26357 269951 269966 50702 50765 76408	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090080	hypogonadotropic hypogonadism 16 with or without anosmia	Sema3a	20346	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2942	bronchiolitis	Adrb2 Ccl11 Cd40 Il17a Il1rn Muc5b	11555 16171 16181 20292 21939 74180	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081211	autosomal recessive intellectual developmental disorder 47	Fmn2	54418	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110289	autosomal recessive limb-girdle muscular dystrophy type 2Y Aliases: LGMD2Y autosomal recessive muscular dystrophy due to LAP1B deficiency autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency muscular dystrophy with progressive weakness, distal contractures and rigid spine muscular dystrophy, limb-girdle, type 2Y	Tor1aip1	208263	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080738	Ehlers-Danlos syndrome spondylodysplastic type 1	B4galt7	218271	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050168	autoimmune polyendocrine syndrome type 2 Aliases: Schmidt syndrome	H2-Aa H2-Ab1 H2-Eb1	14960 14961 14969	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:813	septic arthritis Aliases: infectious arthritis	Cd4	12504	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:850	lung disease	Ace2 Ace Actr2 Adora1 Adora2a Bdkrb2 C3ar1 C5ar1 Ccl2 Cftr Cntn2 Col5a2 Csf3 Ednra Egfr Egr1 F2rl1 Gsn Ifng Il10 Il13 Il15 Il18r1 Il1a Il2 Mmp9 Mpo Muc1 Nos3 Nr3c1 Sftpb Sftpd Tgfb1 Tlr2 Tlr4 Tnf	11421 11539 11540 12062 12267 12273 12638 12832 12985 13617 13649 13653 14063 14815 15978 16153 16163 16168 16175 16182 16183 17395 17523 17829 18127 20296 20388 20390 21367 21803 21898 21926 227753 24088 66713 70008	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11506	suppurative otitis media Aliases: Otitis media with effusion - purulent Purulent otitis media	Ifng Tlr2 Tlr4	15978 21898 24088	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060058	lymphoma Aliases: lymphoid cancer	Chd4 Rela	107932 19697	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1324	lung cancer	Ace Acsl3 Braf Calr Car12 Cftr Chd4 Chrna3 Chrna5 Chrna7 Chrnb4 Clptm1l Comt Csf1r Ctnnb1 Cyp1a1 Dab2ip Dagla Dnmt1 Egfr Erbb2 Ezh2 Fasl Fgf9 Gpx1 Hp Hs3st2 Idh2 Il1r2 Kras Lrp1b Map2k4 Mbd4 Mbl2 Mef2d Mki67 Mlh1 Mmp1a Mpo Mpzl3 Myc Nfkb1 Pik3ca Ptgs2 Rbm10 Rnaset2a Rnaset2b Robo1 Sftpb Slco1b2 Sod2 Stim1 Tnc Tpr Trpc7 Ttr Xrn2	100037283 107932 108015 108989 109880 110834 110835 11421 11441 12317 12387 12638 12846 12978 13076 13433 13649 13866 14056 14103 14180 14775 15439 16178 16653 17193 17195 17261 17345 17350 17523 17869 18033 18706 19225 195646 19876 20388 20656 20866 218335 21923 22139 236732 24128 26398 269060 26946 269951 28253 319742 68195 69601 74205 76459 83995 94217	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2537	inflammatory and toxic neuropathy	Htr2a	15558	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080037	Worth syndrome Aliases: Worth's syndrome autosomal dominant endosteal hyperostosis autosomal dominant osteosclerosis benign form of Worth hyperostosis corticalis generalisata with torus platinus	Lrp5	16973	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090111	PCWH syndrome Aliases: Neurologic Waardenburg-Shah syndrome PCWH Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Hirschsprung disease-Waardenburg syndrome	Mpz	17528	Mus musculus (house mouse)	Alliance of Genome Resources

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